A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7083n100



Internal ID20158699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:12813166..12973587hg38UCSC Ensembl
chr8:12670675..12831096hg19UCSC Ensembl
chr8:12715046..12875467hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38160422
hg19160422
hg18160422
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1028431, nsv1033835
Samples
Known GenesKIAA1456, LINC00681
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7083n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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